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Phenotypic Abnormality (PA): Abnormality of facial musculature

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
+ 1:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
0:   Abnormality of facial musculature [HP:0000301] <12>(2|3) (4|3|0)
- 1:   Abnormality of muscle of facial expression [HP:0430019] <10>(0|0) (0|0|0)
- 1:   Weakness of facial musculature [HP:0030319] <3>(0|1) (1|1|0)
- 1:   Abnormality of jaw muscles [HP:0045037] <2>(2|2) (2|1|0)
- 1:   Abnormality of nasal musculature [HP:0430018] <2>(0|0) (0|0|0)
- 1:   Abnormality of mylohyoid muscle [HP:3000008](0|0) (0|0|0)
- 1:   Abnormality of platysma [HP:3000013](0|0) (0|0|0)
- 1:   Facial hypotonia [HP:0000297](0|0) (1|0|0)
- 1:   Facial muscle hypertrophy [HP:0012892](0|0) (0|0|0)
- 1:   Facial myokymia [HP:0000317](0|0) (0|0|0)
- 1:   Hypomimic face [HP:0000338](0|0) (0|1|0)
- 1:   Hypoplasia of facial musculature [HP:0004660](0|0) (0|0|0)
- 1:   Spasticity of facial muscles [HP:0002491](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Neurotransmitter-gated ion-channel transmembrane pore0.06872Inherited
Nicotinic receptor ligand binding domain-like0.06872Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Kelch motif0.01378Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.0567Inherited
Nicotinic receptor ligand binding domain-like0.0567Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Kelch motif0.01243Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.05229Inherited
Nicotinic receptor ligand binding domain-like0.05229Inherited
ARM repeat0.1213Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.0009149Direct
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.05229Inherited
    48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.07923Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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